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Adhesion proteins meet receptors: a common theme?

机译:粘附蛋白与受体相遇:一个共同的主题?

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Receptors tyrosine kinases (RTKs) and cell adhesion molecules (CAMs) present on the cell surface sense the surrounding environment and influence the fate of cells. For a long time, it was believed that these molecules were working independently and that the sole binding of a ligand was enough to activate the RTK. It is now apparent that there is, in fact, a very tight connection between RTKs and CAMs and that they work in concert. The CAMs influence the activation, the signaling, or the internalization of the RTKs. Some CAMs have similar functions and are therefore interchangeable. CD44 isoforms exemplify the flexibility of these interactions as they can collaborate with several RTKs and can also be substituted by other CAMs with similar functions. In several instances, CAMs not only control the activation of the receptor by presenting the ligand but also regulate the downstream signaling by organizing a signalosome complex. Furthermore, the functions of the CAMs can be controlled by the cellular environment and the binding to their ligands.
机译:细胞表面存在的受体酪氨酸激酶(RTK)和细胞粘附分子(CAM)感知周围环境并影响细胞命运。长期以来,人们认为这些分子是独立工作的,并且配体的唯一结合足以激活RTK。现在很明显,实际上,RTK和CAM之间存在非常紧密的联系,它们可以协同工作。 CAM影响RTK的激活,信令或内部化。一些CAM具有相似的功能,因此可以互换。 CD44亚型体现了这些相互作用的灵活性,因为它们可以与多个RTK协作,也可以被功能相似的其他CAM替代。在几种情况下,CAMs不仅通过提供配体来控制受体的激活,而且通过组织信号体复合物来调节下游信号传导。此外,CAM的功能可以通过细胞环境和与其配体的结合来控制。

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